Canonical Allele Identifier: CA1087852013

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1768907046
• gnomAD v3: 6-35823409-ACACACACACACACACATACATACACACACACATATATATACACACACACACACACACACACACACACACT-A
• gnomAD v4: 6-35823409-ACACACACACACACACATACATACACACACACATATATATACACACACACACACACACACACACACACACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823411_35823480del , CM000668.2:g.35823411_35823480del	GRCh38
NC_000006.11:g.35791188_35791257del , CM000668.1:g.35791188_35791257del	GRCh37
NC_000006.10:g.35899166_35899235del	NCBI36
NG_012184.1:g.23118_23187del
NG_012184.2:g.23118_23187del
NG_012184.3:g.31206_31275del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360215.3:c.*446_*515del MANE Select	ENSP00000353346.1:n.*446_*515del
ENST00000496656.2:n.578+3591_578+3660del
ENST00000651132.1:c.*446_*515del	ENSP00000498322.1:n.*446_*515del
ENST00000651676.1:c.*16+3948_*16+4017del	ENSP00000498699.1:n.*16+3948_*16+4017del
ENST00000651994.1:c.*526_*595del	ENSP00000498310.1:n.*526_*595del
ENST00000652718.1:c.508+3948_508+4017del	ENSP00000498866.1:n.508+3948_508+4017del
ENST00000360215.2:c.*446_*515del	ENSP00000353346.1:n.*446_*515del
ENST00000496656.1:n.812+3591_812+3660del
NM_182548.3:c.*446_*515del	NP_872354.1:n.*446_*515del
NM_182548.4:c.*446_*515del MANE Select	NP_872354.1:n.*446_*515del